"GeneDx"[submitter] AND "HAND2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152441	GRCh38/hg38 4q32.1-35.2(chr4:160757699-190091407)x3	AADAT, ACSL1 +553 more	Copy number gain	See cases	GPathogenic
Select item 59508	GRCh38/hg38 4q34.1-34.3(chr4:171851295-178772816)x1	ADAM29, AGA +85 more	Copy number loss	See cases	GPathogenic
Select item 58061	GRCh38/hg38 4q34.1-35.2(chr4:172200228-189975519)x3	MIR4455, MIR548T +369 more	Copy number gain	See cases	GPathogenic
Select item 1331143	NM_021973.3(HAND2):c.556-18C>G	HAND2	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1263762	NM_021973.3(HAND2):c.153C>G (p.Pro51=)	HAND2, HAND2-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1241341	NC_000004.12:g.173530415G>A	HAND2, HAND2-AS1	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 253675	GRCh37/hg19 4q32.2-34.2(chr4:162344510-177103037)x1	AADAT, ADAM29 +40 more	Copy number loss	See cases	GPathogenic
Select item 253606	GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3	SCOC, SCRG1 +218 more	Copy number gain	See cases	GPathogenic
Select item 253590	GRCh37/hg19 4q28.3-35.1(chr4:136912336-184253252)x3	AADAT, ABCE1 +142 more	Copy number gain	See cases	GPathogenic

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